上海康德弘翼医学临床研究有限公司
临床监查员CRA I
Skills
1 year ago
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Important information
Contract type:
Permanent
Location:
Fuzhou, Fujian, China
Work mode:
Onsite
Published on:
13 August 2026
What they need
该职位来源于猎聘 职责描述:
- Implements and monitors local clinical trials to ensure sponsor and investigator obligations are being met and are compliant with applicable local regulatory requirements and ICH‐GCP guidelines
- Assesses the qualification of potential investigative sites, initiates clinical trials at investigative sites, instructs site personnel on the proper conduct of clinical trials, and close clinical trials at investigative sites
- Reviews and verifies accuracy of clinical trial data collected, either onsite or remotely
- Provides regular site status information to team members, trial management, and updates trial management tool.
- Completes monitoring activity documents as required by Company or Sponsor SOPs or other contractual obligations
- Works closely with other clinical team members to facilitate timely resolution of trial and/or clinical issues
- Escalates site and trial related issues per Company SOPs, until identified issues are resolved or closed
- Performs essential document site file reconciliation
- Performs source document verification and query resolution
- Assesses IP accountability, dispensation, and compliance at the investigative sites
- Verifies Serious Adverse Event (SAE) reporting according to trial specifications and relevant local and ICH GCP guidelines
- Communicates with investigative sites
- Updates applicable tracking systems
- Ensures all required training is completed and documented
- Be assigned logistical support tasks by CTM for Investigator Meetings 任职要求:
- Education
Undergraduate degree or its international equivalent in clinical, science, or health‐related field from an accredited institution; a licensed health‐care professional (i.e., registered nurse); or equivalent work experience required
- Experience
1to 2 years of local trial experience; exposure to MNC and global trials
- Preferred Education and/or Experience
Clinical research experience
Knowledge of ICH and local regulatory authority regulations regarding drug
An advanced degree (e.g., M.S.,M.B.A., PharmD, etc.)
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